Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0140-6736(20)31757-8
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dc.titleEffects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
dc.contributor.authorYoung, Barnaby E
dc.contributor.authorFong, Siew-Wai
dc.contributor.authorChan, Yi-Hao
dc.contributor.authorMak, Tze-Minn
dc.contributor.authorAng, Li Wei
dc.contributor.authorAnderson, Danielle E
dc.contributor.authorLee, Cheryl Yi-Pin
dc.contributor.authorAmrun, Siti Naqiah
dc.contributor.authorLee, Bernett
dc.contributor.authorGoh, Yun Shan
dc.contributor.authorSu, Yvonne CF
dc.contributor.authorWei, Wycliffe E
dc.contributor.authorKalimuddin, Shirin
dc.contributor.authorChai, Louis Yi Ann
dc.contributor.authorPada, Surinder
dc.contributor.authorTan, Seow Yen
dc.contributor.authorSun, Louisa
dc.contributor.authorParthasarathy, Purnima
dc.contributor.authorChen, Yuan Yi Constance
dc.contributor.authorBarkham, Timothy
dc.contributor.authorLin, Raymond Tzer Pin
dc.contributor.authorMaurer-Stroh, Sebastian
dc.contributor.authorLeo, Yee-Sin
dc.contributor.authorWang, Lin-Fa
dc.contributor.authorRenia, Laurent
dc.contributor.authorLee, Vernon J
dc.contributor.authorSmith, Gavin JD
dc.contributor.authorLye, David Chien
dc.contributor.authorNg, Lisa FP
dc.date.accessioned2021-11-30T09:08:45Z
dc.date.available2021-11-30T09:08:45Z
dc.date.issued2020-08-29
dc.identifier.citationYoung, Barnaby E, Fong, Siew-Wai, Chan, Yi-Hao, Mak, Tze-Minn, Ang, Li Wei, Anderson, Danielle E, Lee, Cheryl Yi-Pin, Amrun, Siti Naqiah, Lee, Bernett, Goh, Yun Shan, Su, Yvonne CF, Wei, Wycliffe E, Kalimuddin, Shirin, Chai, Louis Yi Ann, Pada, Surinder, Tan, Seow Yen, Sun, Louisa, Parthasarathy, Purnima, Chen, Yuan Yi Constance, Barkham, Timothy, Lin, Raymond Tzer Pin, Maurer-Stroh, Sebastian, Leo, Yee-Sin, Wang, Lin-Fa, Renia, Laurent, Lee, Vernon J, Smith, Gavin JD, Lye, David Chien, Ng, Lisa FP (2020-08-29). Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study. LANCET 396 (10251) : 603-611. ScholarBank@NUS Repository. https://doi.org/10.1016/S0140-6736(20)31757-8
dc.identifier.issn01406736
dc.identifier.issn1474547X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/208936
dc.description.abstractBackground: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with a 382-nucleotide deletion (∆382) in the open reading frame 8 (ORF8) region of the genome have been detected in Singapore and other countries. We investigated the effect of this deletion on the clinical features of infection. Methods: We retrospectively identified patients who had been screened for the ∆382 variant and recruited to the PROTECT study—a prospective observational cohort study conducted at seven public hospitals in Singapore. We collected clinical, laboratory, and radiological data from patients' electronic medical records and serial blood and respiratory samples taken during hospitalisation and after discharge. Individuals infected with the ∆382 variant were compared with those infected with wild-type SARS-CoV-2. Exact logistic regression was used to examine the association between the infection groups and the development of hypoxia requiring supplemental oxygen (an indicator of severe COVID-19, the primary endpoint). Follow-up for the study's primary endpoint is completed. Findings: Between Jan 22 and March 21, 2020, 278 patients with PCR-confirmed SARS-CoV-2 infection were screened for the ∆382 deletion and 131 were enrolled onto the study, of whom 92 (70%) were infected with the wild-type virus, ten (8%) had a mix of wild-type and ∆382-variant viruses, and 29 (22%) had only the ∆382 variant. Development of hypoxia requiring supplemental oxygen was less frequent in the ∆382 variant group (0 [0%] of 29 patients) than in the wild-type only group (26 [28%] of 92; absolute difference 28% [95% CI 14–28]). After adjusting for age and presence of comorbidities, infection with the ∆382 variant only was associated with lower odds of developing hypoxia requiring supplemental oxygen (adjusted odds ratio 0·07 [95% CI 0·00–0·48]) compared with infection with wild-type virus only. Interpretation: The ∆382 variant of SARS-CoV-2 seems to be associated with a milder infection. The observed clinical effects of deletions in ORF8 could have implications for the development of treatments and vaccines. Funding: National Medical Research Council Singapore.
dc.language.isoen
dc.publisherELSEVIER SCIENCE INC
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectMedicine, General & Internal
dc.subjectGeneral & Internal Medicine
dc.subjectGAMMA
dc.typeArticle
dc.date.updated2021-11-29T03:59:04Z
dc.contributor.departmentDEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL)
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.contributor.departmentMEDICINE
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1016/S0140-6736(20)31757-8
dc.description.sourcetitleLANCET
dc.description.volume396
dc.description.issue10251
dc.description.page603-611
dc.published.statePublished
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